VRT-106 is under clinical development by Guangzhou Virotech Pharmaceutical and currently in Phase I for Cervical Cancer. According to GlobalData, Phase I drugs for Cervical Cancer have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how VRT-106’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

VRT-106 overview

M1-c6v1 is under development for the treatment of advanced or metastatic solid tumor, hepatocellular carcinoma, liver cancer, cervical cancer, triple-negative breast cancer, colorectal cancer, prostate cancer, melanoma and malignant glioma. It is administered through intravenous route. The therapeutic candidate is recombinant oncolytic virus M1 of alpha virus (M1-c6v1).

For a complete picture of VRT-106’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.